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Nasal Vaccine For Smallpox Confers High Levels Of Immunity Without Safety Risks
Scientists at NanoBio 
Corporation and the University of Michigan have demonstrated their nasally   
delivered vaccinia vaccine can protect animals against 77 times the 
potentially lethal dose of smallpox, and without the safety risks of 
current vaccines for smallpox. Vaccinia virus is related to smallpox virus 
and builds immunity against it.
     
The new vaccine confers a high level of safety because it contains  
inactivated vaccinia virus, not the live virus contained in current 
smallpox vaccines, according to the scientists. Live viruses can elicit 
adverse reactions; yet previous attempts to use inactivated virus have 
failed to rouse an adequate immune response against smallpox, the 
scientists said.
 
    
The current study in mice demonstrates that NanoBio's killed-virus 
vaccine elicits a robust immune response because it delivers 
immune-alerting antigens directly to the lining of the nasal mucosa, where 
the virus first enters the body. Immune cells inside the nose immediately 
recognize the foreign invader and quickly build an immune response against 
it, a process known as "mucosal" immunity.
 
    
Mucosal immunity provides a critical first response against respiratory 
viruses, yet injected vaccines do not induce mucosal immunity, said James 
R. Baker Jr., M.D. founder and chairman of NanoBio Corporation. NanoBio is  
a spin-off from the University of Michigan.
 
    
"The key finding is that we have validated in animals a new means of 
immunization that produces a unique and highly effective immune response 
without the potential risks of smallpox vaccination that are no longer  
considered acceptable in the population at large," said Baker.
 
    
"The safety and speed of our nasally delivered vaccine would provide 
the necessary protection to the public in the event of a bioterrorist 
attack or a natural outbreak of a related orthopoxvirus infection such as 
monkeypox," he said.
 
    
Results of the study are published in the February 2008 issue of 
Clinical and Vaccine Immunology. The study is the first to demonstrate 
protective immunity against smallpox using a vaccine with inactivated 
virus, said Baker.
 
    
The data are the latest in a series of preclinical vaccine studies that    
validate NanoBio's patented nanoemulsion platform, a suspension of oil, 
water, alcohol and antimicrobial surfactant together with antigens from 
specific pathogens. The nasally delivered vaccines easily penetrate mucous 
membranes, where dendritic cells engulf the antigen and immediately present 
it to the immune system.
 
    
This rapid awakening of the immune system via mucous membranes negates 
the need for inflammatory stimulants used in traditional injected vaccines, 
which can cause pain and swelling at the site of vaccination, said Baker.
 
    
Animal studies indicate that NanoBio's vaccines quickly trigger robust 
immunity -- without adverse effects -- against a wide array of viruses and 
bacteria, including influenza, hepatitis B, RSV, anthrax and HIV.
 
    
A study to be published this month in the journal AIDS Research and   
Human Retroviruses demonstrates that their HIV vaccine produces both 
mucosal immunity as well as systemic immunity -- the immune system's 
long-term memory that enables it to recognize and combat future infections.
 
    
Both types of immunity are critically important, but developing mucosal 
immunity is particularly valuable in combating sexually transmitted 
diseases because they enter the body through mucous membranes, added Baker. 
Vaccines that are delivered to one mucosal surface, such as inside the 
nose, build immunity at distant mucosal surfaces as well.
 
    
"When you present an infection on one mucosal surface, the immune cells 
that are recruited at that surface also traffic throughout all the mucosal 
surfaces," Baker said. "Our HIV study suggests that the nanoemulsion should 
be evaluated as a mucosal adjuvant for multivalent HIV vaccines."
 
    
Both the HIV and vaccinia vaccine studies demonstrate that vaccinated 
animals developed mucosal and systemic immunity as well as cellular 
immunity, whereby specific immune cells (CD8 and CD4 T cells) were 
successfully primed to recognize and destroy infected cells in the body.
 
    
Cellular immunity kills infected cells in the body and essentially 
removes the infection machinery of the virus. Previous HIV vaccines have 
focused on inducing cellular immunity but not mucosal immunity, said Baker. 
The more types of immunity generated by a vaccine, the higher the level of 
protection and infection-fighting capability the vaccine can provide.
 
    
NanoBio is in various stages of testing its pipeline of nasally 
delivered vaccines. Human testing of the influenza and hepatitis B vaccines 
are being planned, and data from ferret studies on the influenza vaccine 
are expected this quarter.
 
    
About NanoBio
    
NanoBio(R) Corporation is a privately held biopharmaceutical company 
focused on developing and commercializing anti-infective products and 
mucosal vaccines derived from its patented NanoStat(TM) technology 
platform. The company's lead product candidates are topical treatments for 
herpes labialis (cold sores), onychomycosis (nail fungus), MRSA and mucosal 
vaccines for influenza and hepatitis B. The company's headquarters and 
laboratory facilities are located in Ann Arbor, Mich.
 
NanoBio Corporation
http://www.nanobio.com
		
Vaccin nazal pentru vãrsat conferã un nivel ridicat de imunitate, fãrã riscuri de siguranþã - Nasal Vaccine For Smallpox Confers High Levels Of Immunity Without Safety Risks - articole medicale engleza - startsanatate